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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241016Generated: October 30, 2026

2-Amino-5-bromopyridine → Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate

https://huagongshe.com/reaction/241016

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantEthyl isothiocyanatoformateHCID 85320—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl [(5-bromopyridin-2-yl)carbamothioyl]carbamateHCID 5928627470.3%

Reaction Steps

To a solution of 2-amino-5-bromopyridine (5.0 g, 29 mmol) in dioxane (60 mL) was added ethoxycarbonylisothiocyanate (3.4 mL, 29 mmol) in a dropwise manner and the mixture was allowed to stir for 18 h at room temperature. The mixture was then concentrated and the residue triturated with 10% ethyl acetate in hexanes. The solid was collected by filtration and dried to afford ethyl {[(5-bromopyridin-2-yl)amino]carbonothioyl}carbamate (6.2 g, 69%) as a colorless solid. MS (EI) for C9H10BrN3O2S: 305 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-f7ae42fca88149fdbd1c316f268653ce
Source noteuspto-grants-2014_02